Revumenib citrate is under clinical development by Syndax Pharmaceuticals and currently in Phase I for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia). According to GlobalData, Phase I drugs for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia) have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Revumenib citrate’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Revumenib citrate overview
Syndax Pharmaceuticals overview
Syndax Pharmaceuticals (Syndax) is a biopharmaceutical company that discovers, develops and commercializes therapies for multiple cancer indications. The company’s pipeline products include AUGMENT-101-2A for the treatment of R/R KMT2Ar acute lymphoblastic leukemia (ALL), AUGMENT-101-2B treats R/R KMT2Am acute myeloid eukemia (AML); AUGMENT-101-2C for R/R NPM1m Acute Myeloid Leukemia (AML); AUGMENT-102 targets R/R KMT2Ar and NPM1m acute leukemias; BEAT-AML for the treatment of Frontline KMT2Ar and NPM1m Acute Myeloid Leukemia (AML); INTERCEPT for MRD- progression in KMT2Ar and NPM1m acute myeloid leukemia (AML); Colorectal Cancer targets newly diagnosed NPM1m or KMT2Ar acute leukemias; AGAVE-201 treats chronic graft-versus-host disease (GVHD); Idiopathic Pulmonary Fibrosis for idiopathic pulmonary fibrosis. Syndax is headquartered in Waltham, Massachusetts, the US.
For a complete picture of Revumenib citrate’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
